WO2008055013A3 - 5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de la kinase c-fms - Google Patents

5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de la kinase c-fms Download PDF

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Publication number
WO2008055013A3
WO2008055013A3 PCT/US2007/081930 US2007081930W WO2008055013A3 WO 2008055013 A3 WO2008055013 A3 WO 2008055013A3 US 2007081930 W US2007081930 W US 2007081930W WO 2008055013 A3 WO2008055013 A3 WO 2008055013A3
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inhibitors
pyrido
pyrimidines
dihydro
oxo
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PCT/US2007/081930
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WO2008055013A2 (fr
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Mark R Player
William H Parsons
Hui Huang
Daniel A Hutta
Huaping Hu
James Rinker
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Janssen Pharmaceutica Nv
Mark R Player
William H Parsons
Hui Huang
Daniel A Hutta
Huaping Hu
James Rinker
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Application filed by Janssen Pharmaceutica Nv, Mark R Player, William H Parsons, Hui Huang, Daniel A Hutta, Huaping Hu, James Rinker filed Critical Janssen Pharmaceutica Nv
Publication of WO2008055013A2 publication Critical patent/WO2008055013A2/fr
Publication of WO2008055013A3 publication Critical patent/WO2008055013A3/fr

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
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    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

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  • Health & Medical Sciences (AREA)
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  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
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  • General Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Neurology (AREA)
  • Heart & Thoracic Surgery (AREA)
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  • Biomedical Technology (AREA)
  • Pulmonology (AREA)
  • Hospice & Palliative Care (AREA)
  • Virology (AREA)
  • Urology & Nephrology (AREA)
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Abstract

L'invention traite du besoin actuel en inhibiteurs sélectifs et puissants de protéine tyrosine kinase en proposant des inhibiteurs puissants de la kinase c-fms. L'invention porte sur les nouveaux composés représentés par la Formule I : ou un sel, un stéréoisomère, un tautomère, un dérivé cristallin, un dérivé polymorphe, un dérivé amorphe, un solvate, un hydrate, un ester, un promédicament ou une forme métabolite de celui-ci, et où A, Y, Z, R101 et R200 sont décrits dans la revendication.
PCT/US2007/081930 2006-10-31 2007-10-19 5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de la kinase c-fms WO2008055013A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85552306P 2006-10-31 2006-10-31
US60/855,523 2006-10-31

Publications (2)

Publication Number Publication Date
WO2008055013A2 WO2008055013A2 (fr) 2008-05-08
WO2008055013A3 true WO2008055013A3 (fr) 2009-01-22

Family

ID=39144475

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2007/081930 WO2008055013A2 (fr) 2006-10-31 2007-10-19 5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de la kinase c-fms

Country Status (4)

Country Link
US (1) US20080114007A1 (fr)
AR (1) AR063723A1 (fr)
CL (1) CL2007003163A1 (fr)
WO (1) WO2008055013A2 (fr)

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7642270B2 (en) * 2005-09-14 2010-01-05 Janssen Pharmaceutica N.V. 5-oxo-5,8-dihydro-pyrido-pyrimidine as inhibitors of c-fms kinase
BRPI1015135B1 (pt) 2009-06-29 2021-08-03 Incyte Holdings Corporation Pirimidinonas inibidoras de pi3k, composição compreendendo tais compostos, bem como usos dos mesmos
WO2011075643A1 (fr) * 2009-12-18 2011-06-23 Incyte Corporation Dérivés condensés d'hétéroaryles substitués à titre d'inhibiteurs de pi3k
AR079529A1 (es) * 2009-12-18 2012-02-01 Incyte Corp Derivados arilo y heteroarilo sustituidos y fundidos como inhibidores de la pi3k
FR2955109B1 (fr) * 2010-01-08 2012-09-07 Sanofi Aventis Derives de 5-oxo-5,8-dihydro-pyrido[2, 3-d]pyrimidine, leur preparation et leur application en therapeutique
EP2558463A1 (fr) 2010-04-14 2013-02-20 Incyte Corporation Dérivés condensés en tant qu'inhibiteurs de i3
US9062055B2 (en) 2010-06-21 2015-06-23 Incyte Corporation Fused pyrrole derivatives as PI3K inhibitors
WO2012087881A1 (fr) 2010-12-20 2012-06-28 Incyte Corporation N-(1-(phényl substitué)éthyl)-9h-purin-6-amines en tant qu'inhibiteurs de pi3k
US9108984B2 (en) 2011-03-14 2015-08-18 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as PI3K inhibitors
US9126948B2 (en) 2011-03-25 2015-09-08 Incyte Holdings Corporation Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
US8518214B2 (en) 2011-07-18 2013-08-27 Nalco Company Debonder and softener compositions
ES2722524T3 (es) 2011-09-02 2019-08-13 Incyte Holdings Corp Heterociclaminas como inhibidores de pi3k
JP2014530867A (ja) 2011-10-20 2014-11-20 アッヴィ・インコーポレイテッド キナーゼのピリドピリミジノン阻害剤
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
CN104428282B (zh) 2012-07-12 2017-10-20 日产化学工业株式会社 肟取代酰胺化合物和有害生物防除剂
WO2015019037A1 (fr) * 2013-08-05 2015-02-12 Almac Discovery Limited Composés pharmaceutiques
GB201315486D0 (en) * 2013-08-30 2013-10-16 Ucb Pharma Sa Antibodies
WO2015191677A1 (fr) 2014-06-11 2015-12-17 Incyte Corporation Dérivés d'hétéroarylaminoalkylphényle bicycliques à titre d'inhibiteurs de pi3k
MD3831833T2 (ro) 2015-02-27 2023-04-30 Incyte Holdings Corp Procedee pentru prepararea unui inhibitor PI3K
US9988401B2 (en) 2015-05-11 2018-06-05 Incyte Corporation Crystalline forms of a PI3K inhibitor
US9732097B2 (en) 2015-05-11 2017-08-15 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
CN105130986B (zh) * 2015-09-30 2017-07-18 广州科擎新药开发有限公司 嘧啶或吡啶并吡啶酮类化合物及其应用
EP3877380A1 (fr) 2018-11-05 2021-09-15 Syngenta Participations Ag Composés azole-amide à action pesticide
WO2020191503A1 (fr) * 2019-03-27 2020-10-01 Algernon Pharmaceuticals Inc. Procédés et utilisations de bromantane et de dérivés de celui-ci pour le traitement d'une maladie pulmonaire, d'une stéatose hépatique et de troubles rénaux
CN112457309B (zh) * 2020-09-01 2023-03-17 扬州工业职业技术学院 一种苯基取代吡啶并嘧啶胺类化合物及其作为抗菌药物的应用

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09221424A (ja) * 1995-12-13 1997-08-26 Dainippon Pharmaceut Co Ltd 抗腫瘍剤
WO2001070741A1 (fr) * 2000-03-06 2001-09-27 Warner-Lambert Company Inhibiteurs de tyrosine kinase a base de 5-alkylpyrido[2,3-d]pyrimidines
WO2007033232A1 (fr) * 2005-09-14 2007-03-22 Janssen Pharmaceutica, N.V. 5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de kinase c-fms

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004096795A2 (fr) * 2003-04-25 2004-11-11 3-Dimensional Pharmaceuticals, Inc. Inhibiteurs de la kinase c-fms
US7642270B2 (en) * 2005-09-14 2010-01-05 Janssen Pharmaceutica N.V. 5-oxo-5,8-dihydro-pyrido-pyrimidine as inhibitors of c-fms kinase

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09221424A (ja) * 1995-12-13 1997-08-26 Dainippon Pharmaceut Co Ltd 抗腫瘍剤
WO2001070741A1 (fr) * 2000-03-06 2001-09-27 Warner-Lambert Company Inhibiteurs de tyrosine kinase a base de 5-alkylpyrido[2,3-d]pyrimidines
WO2007033232A1 (fr) * 2005-09-14 2007-03-22 Janssen Pharmaceutica, N.V. 5-oxo-5,8-dihydro-pyrido-pyrimidines comme inhibiteurs de kinase c-fms

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 199747, Derwent World Patents Index; AN 1997-506304, XP002472582 *

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Publication number Publication date
CL2007003163A1 (es) 2008-06-27
US20080114007A1 (en) 2008-05-15
AR063723A1 (es) 2009-02-11
WO2008055013A2 (fr) 2008-05-08

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